Canonical Allele Identifier: CA400179862

Gene: SGCA

Linked Data

• gnomAD v4: 17-50168419-A-T
• MyVariant Identifiers: chr17:g.48245780A>T (hg19) ; chr17:g.50168419A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50168419A>T , CM000679.2:g.50168419A>T	GRCh38
NC_000017.10:g.48245780A>T , CM000679.1:g.48245780A>T	GRCh37
NC_000017.9:g.45600779A>T	NCBI36
NG_008889.1:g.7415A>T , LRG_203:g.7415A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504073.2:c.431A>T	ENSP00000422030.2:p.Asp144Val
ENST00000511303.6:n.156A>T
ENST00000512526.2:c.422A>T	ENSP00000426606.2:n.422A>T
ENST00000682109.1:c.311A>T	ENSP00000508041.1:p.Asp104Val
ENST00000683226.1:n.141A>T
ENST00000683294.1:c.431A>T	ENSP00000508134.1:p.Asp144Val
ENST00000262018.8:c.431A>T MANE Select	ENSP00000262018.3:p.Asp144Val
ENST00000262018.7:c.431A>T	ENSP00000262018.3:p.Asp144Val
ENST00000344627.10:c.431A>T	ENSP00000345522.6:p.Asp144Val
ENST00000502555.5:c.*90A>T	ENSP00000422817.1:n.*90A>T
ENST00000511303.5:c.152A>T	ENSP00000426104.1:p.Asp51Val
ENST00000512526.1:c.266A>T
ENST00000513821.5:c.431A>T	ENSP00000426571.1:p.Asp144Val
ENST00000513942.5:n.222A>T
ENST00000514934.1:c.*137A>T	ENSP00000423168.1:n.*137A>T
NM_000023.2:c.431A>T , LRG_203t1:c.431A>T	NP_000014.1:p.Asp144Val
NM_001135697.1:c.431A>T	NP_001129169.1:p.Asp144Val
XM_011525120.1:c.431A>T	XP_011523422.1:p.Asp144Val
XM_011525121.1:c.431A>T	XP_011523423.1:p.Asp144Val
XM_011525122.1:c.431A>T	XP_011523424.1:p.Asp144Val
XM_011525123.1:c.431A>T	XP_011523425.1:p.Asp144Val
XM_011525124.1:c.125A>T	XP_011523426.1:p.Asp42Val
XR_934517.1:n.497A>T
NM_000023.3:c.431A>T	NP_000014.1:p.Asp144Val
NM_001135697.2:c.431A>T	NP_001129169.1:p.Asp144Val
NR_135553.1:n.487A>T
XM_011525120.2:c.593A>T	XP_011523422.2:p.Asp198Val
XM_011525121.2:c.593A>T	XP_011523423.2:p.Asp198Val
XM_011525122.2:c.593A>T	XP_011523424.2:p.Asp198Val
XM_011525123.2:c.593A>T	XP_011523425.2:p.Asp198Val
XM_011525124.2:c.125A>T	XP_011523426.1:p.Asp42Val
XM_024450873.1:c.125A>T	XP_024306641.1:p.Asp42Val
XR_002958056.1:n.949A>T
NM_000023.4:c.431A>T MANE Select	NP_000014.1:p.Asp144Val
NM_001135697.3:c.431A>T	NP_001129169.1:p.Asp144Val
NR_135553.2:n.467A>T